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在三乙基硼存在下制备鳕鱼胶原蛋白与丙烯酸丁酯和乙烯基丁基醚的接枝共聚物——在再生医学中的应用前景

Production of Graft Copolymers of Cod Collagen with Butyl Acrylate and Vinyl Butyl Ether in the Presence of Triethylborane-Prospects for Use in Regenerative Medicine.

作者信息

Semenycheva Lyudmila, Chasova Victoria O, Pegeev Nikita L, Uromicheva Marina A, Mitin Alexander V, Kuznetsova Yulia L, Farafontova Ekaterina A, Rubtsova Yulia P, Linkova Daria D, Egorikhina Marfa N

机构信息

Faculty of Chemistry, National Research Lobachevsky State University of Nizhny Novgorod, 23, Gagarin Ave., 603022 Nizhny Novgorod, Russia.

Federal State Budgetary Educational Institution of Higher Education, Privolzhsky Research Medical University of the Ministry of Health of the Russian Federation, 603005 Nizhny Novgorod, Russia.

出版信息

Polymers (Basel). 2023 Jul 25;15(15):3159. doi: 10.3390/polym15153159.

DOI:10.3390/polym15153159
PMID:37571053
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10421105/
Abstract

Collagen is a suitable material for regenerative medicine because it is characterized by its good biocompatibility. However, due to its fibrillar structure, it cannot organize itself into three-dimensional porous structures without additional modification. The introduction of synthetic monomer elements into the collagen macromolecules is a technique used to form three-dimensional, collagen-based, branched, and crosslinked structures. New types of graft copolymers made from cod collagen with a butyl acrylate and vinyl butyl ether copolymer in aqueous dispersion were obtained in the presence of triethylborane by a radical mechanism. The process of graft copolymer formation proceeded as usual by radical initiation, through radicals formed during triethylborane oxidation by oxygen residues, collagen borination, and reversible inhibition with the participation of a boroxyl radical. The characteristics of the graft copolymers were determined using methods of physical and chemical analysis (GPC, SEM, IR spectroscopy, etc.), while the cytotoxicity was assessed using the MTT assay method. It is shown that the grafting of alternating blocks of butyl acrylate and vinyl butyl ether to the protein macromolecules results in changes in the morphological pattern of the graft co-polymer in comparison with native collagen. This is manifested in the development of consolidations around the collagen fibers of the structural matrices, with the co-polymer cellular structure consisting of interpenetrating pores of unequal size. Additionally, it is important that the graft co-polymer solutions are not toxic at a certain concentration. The above properties confirm the promising nature of the technique's application as the basis for producing new materials for regenerative medicine.

摘要

胶原蛋白是再生医学的合适材料,因为它具有良好的生物相容性。然而,由于其纤维状结构,未经额外修饰时它无法自行组织成三维多孔结构。将合成单体元素引入胶原蛋白大分子是一种用于形成三维、基于胶原蛋白的、分支和交联结构的技术。在三乙基硼烷存在下,通过自由基机理,由鳕鱼胶原蛋白与丙烯酸丁酯和乙烯基丁基醚共聚物在水分散体中制得新型接枝共聚物。接枝共聚物的形成过程像往常一样通过自由基引发进行,通过三乙基硼烷被氧残基氧化、胶原蛋白硼化以及硼氧基自由基参与的可逆抑制过程中形成的自由基。使用物理和化学分析方法(凝胶渗透色谱法、扫描电子显微镜、红外光谱等)测定接枝共聚物的特性,同时使用MTT测定法评估细胞毒性。结果表明,与天然胶原蛋白相比,丙烯酸丁酯和乙烯基丁基醚交替嵌段接枝到蛋白质大分子上会导致接枝共聚物的形态模式发生变化。这表现为在结构基质的胶原纤维周围形成固结,共聚物的细胞结构由大小不等的互穿孔隙组成。此外,重要的是接枝共聚物溶液在一定浓度下无毒。上述特性证实了该技术作为生产再生医学新材料基础的应用前景。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b29b/10421105/76e7a8ef7116/polymers-15-03159-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b29b/10421105/c140cea6cf02/polymers-15-03159-sch001.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b29b/10421105/2b82a91cb387/polymers-15-03159-sch002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b29b/10421105/817b0afb8901/polymers-15-03159-sch003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b29b/10421105/c4bc730ea311/polymers-15-03159-sch004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b29b/10421105/47b0daaaa762/polymers-15-03159-sch005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b29b/10421105/dc2052164287/polymers-15-03159-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b29b/10421105/603cf99c8476/polymers-15-03159-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b29b/10421105/51895361850a/polymers-15-03159-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b29b/10421105/2e2245fe8a79/polymers-15-03159-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b29b/10421105/816c0e27b7ec/polymers-15-03159-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b29b/10421105/76e7a8ef7116/polymers-15-03159-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b29b/10421105/c140cea6cf02/polymers-15-03159-sch001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b29b/10421105/d8f77ef94cf3/polymers-15-03159-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b29b/10421105/2b82a91cb387/polymers-15-03159-sch002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b29b/10421105/817b0afb8901/polymers-15-03159-sch003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b29b/10421105/c4bc730ea311/polymers-15-03159-sch004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b29b/10421105/47b0daaaa762/polymers-15-03159-sch005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b29b/10421105/dc2052164287/polymers-15-03159-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b29b/10421105/603cf99c8476/polymers-15-03159-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b29b/10421105/51895361850a/polymers-15-03159-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b29b/10421105/2e2245fe8a79/polymers-15-03159-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b29b/10421105/816c0e27b7ec/polymers-15-03159-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b29b/10421105/76e7a8ef7116/polymers-15-03159-g007.jpg

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